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Dimercaprol
Pronunciation
U.S. Brand Names
Generic Available
Synonyms
Pharmacological Index
Use
Pregnancy Risk Factor
Contraindications
Warnings/Precautions
Adverse Reactions
Drug Interactions
Stability
Mechanism of Action
Pharmacodynamics/Kinetics
Usual Dosage
Administration
Test Interactions
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Dental Health: Local Anesthetic/Vasoconstrictor Precautions
Dental Health: Effects on Dental Treatment
Patient Information
Nursing Implications
Dosage Forms
References

Pronunciation
(dye mer KAP role)

U.S. Brand Names
BAL in Oil®

Generic Available

No


Synonyms
BAL; British Anti-Lewisite; Dithioglycerol

Pharmacological Index

Antidote


Use

Antidote to gold, arsenic (except arsine), and mercury poisoning (except nonalkyl mercury); adjunct to edetate calcium disodium in lead poisoning; possibly effective for antimony, bismuth, chromium, copper, nickel, tungsten, or zinc


Pregnancy Risk Factor

C


Contraindications

Hepatic insufficiency (unless due to arsenic poisoning); do not use on iron, cadmium, or selenium poisoning


Warnings/Precautions

Potentially a nephrotoxic drug, use with caution in patients with oliguria or glucose 6-phosphate dehydrogenase deficiency; keep urine alkaline to protect kidneys; administer all injections deep I.M. at different sites


Adverse Reactions

>10%:

Cardiovascular: Hypertension, tachycardia (dose-related)

Central nervous system: Headache

1% to 10%: Gastrointestinal: Nausea, vomiting

<1%: Nervousness, fever, convulsions, salivation, transient neutropenia, thrombocytopenia, increased PT, pain at the injection site, abscess formation, myalgia, paresthesia, blepharospasm, burning eyes, nephrotoxicity, dysuria, burning sensation of the lips, mouth, throat, and penis


Drug Interactions

Toxic complexes with iron, cadmium, selenium, or uranium


Stability

Do not mix in the same syringe with edetate calcium disodium


Mechanism of Action

Sulfhydryl group combines with ions of various heavy metals to form relatively stable, nontoxic, soluble chelates which are excreted in urine


Pharmacodynamics/Kinetics

Distribution: Distributes to all tissues including the brain

Metabolism: Rapidly to inactive products

Time to peak serum concentration: 0.5-1 hour

Elimination: In urine


Usual Dosage

Children and Adults: Deep I.M.:

Lead poisoning (in conjunction with calcium EDTA): For symptomatic acute encephalopathy or blood level >100 mcg/dL: 4-5 mg/kg every 4 hours for 3-5 days


Administration

Administer deep I.M. only


Test Interactions

Iodine 131I thyroidal uptake values may be decreased


Mental Health: Effects on Mental Status

May cause nervousness


Mental Health: Effects on Psychiatric Treatment

May produce neutropenia; use caution with clozapine and carbamazepine


Dental Health: Local Anesthetic/Vasoconstrictor Precautions

No information available to require special precautions


Dental Health: Effects on Dental Treatment

No effects or complications reported


Patient Information

Frequent blood and urine tests may be required


Nursing Implications

Urine should be kept alkaline because chelate dissociates in acid media


Dosage Forms

Injection: 100 mg/mL (3 mL)


References

Cantilena LR Jr and Klaassen CD, "The Effect of Chelating Agents on the Excretion of Endogenous Metals," Toxicol Appl Pharmacol, 1982, 63(3):344-50.

Kosnett MJ, "Unanswered Questions in Metal Chelation," J Toxicol Clin Toxicol, 1992, 30(4):529-47.

"Treatment Guidelines for Lead Exposure in Children. American Academy of Pediatrics Committee on Drugs," Pediatrics, 1995, 96(1 Pt 1):155-60.


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